CN101934230A - Iron inner electrolysis catalyst and preparation method thereof - Google Patents
Iron inner electrolysis catalyst and preparation method thereof Download PDFInfo
- Publication number
- CN101934230A CN101934230A CN 201010261523 CN201010261523A CN101934230A CN 101934230 A CN101934230 A CN 101934230A CN 201010261523 CN201010261523 CN 201010261523 CN 201010261523 A CN201010261523 A CN 201010261523A CN 101934230 A CN101934230 A CN 101934230A
- Authority
- CN
- China
- Prior art keywords
- molecular sieve
- iron
- copper
- preparation
- manganese dioxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Catalysts (AREA)
- Water Treatment By Electricity Or Magnetism (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
Abstract
The invention relates to catalysts for treating industrial waste water, in particular to an iron inner electrolysis catalyst and a preparation method thereof. The iron inner electrolysis catalyst comprises the following components: simple copper supported by molecular sieves, manganese dioxide supported by molecular sieves, and natural manganese ore with the mass ratio thereof being 1:0.5-1.0:0.5-1.0. The preparation method thereof comprises the following steps: respectively immersing roasted molecular sieves in the solutions of soluble copper salt and manganese salt by the supporting capacity of copper and manganese dioxide; dipping, drying and roasting the molecular sieves to respectively obtain the copper oxide and manganese dioxide supported by the molecular sieves; crushing and sieving the natural manganese ore to obtain the natural manganese ore granules; reducing the copper oxide supported by the molecular sieves by using hydrogen to obtain the simple copper supported by the molecular sieves; and mixing the simple copper supported by molecular sieves, manganese dioxide supported by molecular sieves, and natural manganese ore granules by the mass ratio to obtain the product. Accordingly, the invention is suitable for the pre-treatment before the biochemical treatment of high-chromaticity non-biodegradable industrial waste water.
Description
Technical field
The present invention relates to a kind of catalyst that is used to handle industrial wastewater, especially relate to a kind of internal electrolysis of iron Catalysts and its preparation method.
Background technology
In recent years, along with the pollution of industrial wastewaters such as dyeing and finishing, chemical industry, plating to peripheral water body and soil increases day by day, particularly often contain toxic big dye well intermediate in the dyeing and finishing wastewater, also contain the combustion adjuvant of bio-refractory and acid, alkali, inorganic salts etc. simultaneously.The water yield of this type of industrial wastewater is big, colourity is high, CODcr content height, and biochemical degradability is poor, compares with city domestic sewage, and difficulty of governance is bigger.At present, to this class processing method of industrial waste water often with the preliminary treatment of physico-chemical process as biochemical process.There are problems such as the high and technical difficulty of disposal cost is big in physico-chemical process.Therefore, seeking a kind of effective preprocess method, improve the biodegradability that biochemical bacteria is had the hardly degraded organic substance that suppresses poisoning effect, is the key issue that improves this class biochemical treatment of industrial wastewater.
The internal electrolysis of iron preconditioning technique that find the seventies in 20th century is in acid solution, can form numerous small galvanic cell between iron filings and the carbon granule, by the nascent state Fe that generates
2+With the H atom some oxidation state organic matter is reduced into ortho states, and makes the cracking of part difficult degradation ring-type organic matter, generate the easily open loop organic matter of degraded, thereby improve the biodegradability of dyeing waste water.While Fe
2+Have good flocculation, can be with the organic matter adsorbing separation in the waste water, therefore, these advantages make this method be subjected to general attention both at home and abroad as the preliminary treatment of treatment of dyeing wastewater.Yet also there are many shortcomings in this method: (1) uses iron after a period of time, charcoal to be easy to harden, and produces channel and influences its treatment effect; (2) oxidation-reduction potential between iron～carbon resistance rod is less, influences organic molecule in interelectrode redox reaction; (3) efficient of electrolytic treatments waste water is not high in the iron charcoal.At electrolysis tech in traditional iron～charcoal, Chinese patent CN101671067 discloses a kind of method with gas, water backwashing electrolysis filler in catalytic iron, overcomes the problem that iron～charcoal is easy to harden; Chinese patent CN02111901 discloses a kind of with the alternative iron carbon resistance rod of iron～copper electrode, improves the potential difference of two interpolars, further improved electrochemical reaction efficiency, yet this patent proposes to have difficulties aspect the process implementing as copper electrode with the copper frame.Chinese patent CN1935680 discloses and has used iron plane flower and the copper turnings microelectrode material as catalytic internal electrolysis of iron, but during the extensive application of kind electrode material, rare copper turnings is also hard-earned; Chinese patent CN101641068 further proposes, and uses a kind of copper-plated magnetic iron oxide powdery particulate to substitute carbon resistance rod, has solved the copper microelectrode and has reclaimed problem.
In catalytic internal electrolysis of iron, Chinese patent CN1382649 proposes the zeolite of application load 3%～4% cationic surfactant modification as the catalyst in the electrolysis in catalysis iron～copper.The zeolite that in Chinese patent CN1468810, also adopts 0～10% cationic surfactant modification similarly as Catalyzed Aluminum in the catalyst of electrolytic treatments sewage.
Summary of the invention
The object of the present invention is to provide a kind of internal electrolysis of iron Catalysts and its preparation method that is used to handle industrial wastewater.
It consists of molecular sieve carried elemental copper, molecular sieve carried manganese dioxide and natural manganese sand internal electrolysis of iron catalyst of the present invention, and the mass ratio of each component is molecular sieve carried elemental copper: molecular sieve carried manganese dioxide: natural manganese sand=1: (0.5～1.0): (0.5～1.0).
The load capacity of copper can be 1%～20% in the described molecular sieve carried elemental copper.
The load capacity of manganese dioxide can be 1%～25% in the described molecular sieve carried manganese dioxide.
Described natural manganese sand can be manganese ore etc., and its manganese dioxide content can be 25%～45%.
Described molecular sieve can be Si-Al zeolite molecular sieve etc., especially 4A Si-Al zeolite molecular sieve etc.
Described internal electrolysis of iron Preparation of catalysts method may further comprise the steps:
1) with standby after the molecular sieve roasting;
2) load capacity by copper and manganese dioxide immerses molecular sieve in soluble copper salt and the manganese salt solution respectively, drain behind the dipping, and drying, molecular sieve carried cupric oxide and molecular sieve carried manganese dioxide are made in roasting respectively;
3), get the natural manganese sand particle with natural manganese sand fragmentation, screening;
4) with molecular sieve carried cupric oxide hydrogen reducing, obtain molecular sieve carried elemental copper;
5) be molecular sieve carried elemental copper with molecular sieve carried elemental copper, molecular sieve carried manganese dioxide and natural manganese sand by mass ratio: molecular sieve carried manganese dioxide: natural manganese sand=1: (0.5～1.0): (0.5～1.0) mixes and promptly gets the internal electrolysis of iron catalyst.
In step 1), the temperature of described roasting can be 450～550 ℃.
In step 2) in, the concentration of described soluble copper salt can be 0.1～1.0mol/L, and the concentration of described manganese salt solution can be 0.1～1.0mol/L; The time of described dipping can be 2～30min, and the temperature of described drying can be 100～130 ℃, and the temperature of described roasting can be 200～300 ℃.
In step 3), described natural manganese sand particle grain size can be 2～5mm.
Si-Al zeolite molecular sieve used in the present invention has big specific area and special cage structure, as carrier loaded copper and manganese, can make copper, manganese high degree of dispersion at carrier surface.And molecular sieve carried high dispersing copper distribution of particles is in the space of iron plane flower and copper facing iron plane flower, increase the specific surface of tough cathode greatly, thereby improve the reducing power of anode iron in the catalytic internal electrolysis of iron Industrial Wastewater Treatment process and the oxidability on tough cathode surface, in addition, the adsorption capacity that molecular sieve is stronger, organic matter in the waste water can be enriched in the molecular sieve surface, thereby strengthen copper organic oxidative degradation performance.Molecular sieve carried manganese dioxide-catalyst and natural manganese sand by to the organic absorption in the waste water, electronics transfer, desorption, make organic matter degradation in the processing procedure of catalytic internal electrolysis of iron industrial wastewater.
Organic matter (HA) in the manganese dioxide absorption waste water on the molecular sieve surface of load and manganese sand surface by to organic oxidation, makes organic matter degradation, organic matter after the degraded and Mn
IIDesorption and to solution diffusion, Mn
IIBe oxidized to manganese dioxide by the oxygen in the water, be deposited on the surface of solids, return to initial state, form a catalytic cycle, strengthen the ability that catalytic internal electrolysis of iron is handled industrial wastewater effectively.
Adopt prepared catalyst of the present invention and iron plane flower, copper facing iron plane flower to form the catalytic internal electrolysis of iron filtrate, catalytic internal electrolysis of iron is handled the dyeing waste water of bio-refractory, can obtain good pretreating effect.When the time of staying was 30～60min, the colourity of dyeing waste water and CODcr clearance reached respectively more than 70% and 50%, were suitable as the biochemical treatment of industrial wastewater preliminary treatment before of colourity height, difficult for biological degradation.
The specific embodiment
The invention will be further described below by embodiment.
The handled industrial wastewater of following embodiment is a dyeing waste water, and the colourity of former water is 650, and CODcr is 1623mg/L, pH=12.
Embodiment 1
1) getting 100g respectively, respectively to immerse copper nitrate solution and the 500ml concentration that 500ml concentration is 0.5mol/L through the 4A Si-Al zeolite molecular sieve that 500 ℃ of calcination process are crossed be in the manganese nitrate solution of 0.6mol/L, drain behind the dipping 30min, at 110 ℃ of dry 5h, and, obtain the copper load capacity and be 12% molecular sieve carried cupric oxide and manganese dioxide load amount and be 14% molecular sieve carried manganese dioxide at 300 ℃ of roasting 3h.
2) molecular sieve carried cupric oxide uses preceding with 3% (H
2/ N
2, v/v) gaseous mixture is at 230 ℃ of reductase 12 .5h, after obtain molecular sieve carried elemental copper.
3) natural manganese sand through Mechanical Crushing, sieve out grain through the particle of 2～5mm.
4) with iron plane flower 50g, copper facing iron plane flower 20g, molecular sieve carried elemental copper 5g, molecular sieve carried manganese dioxide 5g, contain the natural manganese sand 5g of manganese dioxide 25%, mix the back and form the catalytic internal electrolysis of iron filtrate, regulate the acidity of dyeing waste water with 1mol/L sulfuric acid, make pH=5, the processing time is 60min.After catalytic internal electrolysis of iron is handled, the colourity 150 of water outlet, chroma removal rate 77%, CODcr=631, CODcr clearance are 61.1%.
Embodiment 2
The load capacity for preparing copper by the preparation method of embodiment 1 is that 20% molecular sieve carried elemental copper and manganese dioxide load amount are 25% molecular sieve carried manganese dioxide.
With iron plane flower 50g, copper facing iron plane flower 20g, molecular sieve carried elemental copper 5g, molecular sieve carried manganese dioxide 4g, the natural manganese sand 4g that contains manganese dioxide 30% evenly mixes the back and forms the catalytic internal electrolysis of iron filtrate, regulate the acidity of dyeing waste water with 1mol/L sulfuric acid, make pH=5, the processing time is 60min.After catalytic internal electrolysis of iron is handled, the colourity 160 of water outlet, chroma removal rate 75%, CODcr=670, CODcr clearance are 58.7%.
Embodiment 3
The load capacity for preparing copper by the preparation method of embodiment 1 is that 5% molecular sieve carried elemental copper and manganese dioxide load amount are 20% molecular sieve carried manganese dioxide.
With iron plane flower 50g, copper facing iron plane flower 20g, molecular sieve carried elemental copper 5g, molecular sieve carried manganese dioxide 5g, the natural manganese sand 5g that contains manganese dioxide 45%, evenly mix the back and form the catalytic internal electrolysis of iron filtrate, regulate the acidity of dyeing waste water with 1mol/L sulfuric acid, make pH=5, the processing time is 60min.After catalytic internal electrolysis of iron is handled, the colourity 175 of water outlet, chroma removal rate 73%, CODcr=765, CODcr clearance are 52.8%.
Embodiment 4
The load capacity for preparing copper by the preparation method of embodiment 1 is that 10% molecular sieve carried elemental copper and manganese dioxide load amount are 5% molecular sieve carried manganese dioxide.
With iron plane flower 50g, copper facing iron plane flower 20g, molecular sieve carried elemental copper 5g, molecular sieve carried manganese dioxide 5g, the natural manganese sand 5g that contains manganese dioxide 25%, evenly mix the back and form the catalytic internal electrolysis of iron filtrate, regulate the acidity of dyeing waste water with 1mol/L sulfuric acid, make pH=5, the processing time is 60min.After catalytic internal electrolysis of iron is handled, the colourity 180 of water outlet, chroma removal rate 72%, CODcr=805, CODcr clearance are 50.4%.
Embodiment 5
The load capacity for preparing copper by the preparation method of embodiment 1 is that 12% molecular sieve carried elemental copper and manganese dioxide load amount are 25% molecular sieve carried manganese dioxide.
With iron plane flower 50g, copper facing iron plane flower 20g, molecular sieve carried elemental copper 5g, molecular sieve carried manganese dioxide 2.5g, the natural manganese sand 2.5g that contains manganese dioxide 30%, evenly mix the back and form the catalytic internal electrolysis of iron filtrate, regulate the acidity of dyeing waste water with 1mol/L sulfuric acid, make pH=5, the processing time is 30min.After catalytic internal electrolysis of iron is handled, the colourity 175 of water outlet, chroma removal rate 73%, CODcr=800, CODcr clearance are 50.7%.
Claims (10)
1. internal electrolysis of iron Catalysts and its preparation method, it is characterized in that it consists of molecular sieve carried elemental copper, molecular sieve carried manganese dioxide and natural manganese sand, the mass ratio of each component is molecular sieve carried elemental copper: molecular sieve carried manganese dioxide: natural manganese sand=1: (0.5～1.0): (0.5～1.0).
2. internal electrolysis of iron Catalysts and its preparation method as claimed in claim 1 is characterized in that the load capacity of copper in the described molecular sieve carried elemental copper is 1%～20%.
3. internal electrolysis of iron Catalysts and its preparation method as claimed in claim 1 is characterized in that the load capacity of manganese dioxide in the described molecular sieve carried manganese dioxide is 1%～25%.
4. internal electrolysis of iron Catalysts and its preparation method as claimed in claim 1 is characterized in that described natural manganese sand is a manganese ore, and its manganese dioxide content is 25%～45%.
5. internal electrolysis of iron Catalysts and its preparation method as claimed in claim 1 is characterized in that described molecular sieve is the Si-Al zeolite molecular sieve.
6. internal electrolysis of iron Catalysts and its preparation method as claimed in claim 5 is characterized in that described Si-Al zeolite molecular sieve is a 4A Si-Al zeolite molecular sieve.
7. described internal electrolysis of iron Preparation of catalysts method as claimed in claim 1 is characterized in that may further comprise the steps:
1) with standby after the molecular sieve roasting;
2) load capacity by copper and manganese dioxide immerses molecular sieve in soluble copper salt and the manganese salt solution respectively, drain behind the dipping, and drying, molecular sieve carried cupric oxide and molecular sieve carried manganese dioxide are made in roasting respectively;
3), get the natural manganese sand particle with natural manganese sand fragmentation, screening;
4) with molecular sieve carried cupric oxide hydrogen reducing, obtain molecular sieve carried elemental copper;
5) be molecular sieve carried elemental copper with molecular sieve carried elemental copper, molecular sieve carried manganese dioxide and natural manganese sand by mass ratio: molecular sieve carried manganese dioxide: natural manganese sand=1: (0.5～1.0): (0.5～1.0) mixes and promptly gets the internal electrolysis of iron catalyst.
8. described internal electrolysis of iron Preparation of catalysts method as claimed in claim 7 is characterized in that in step 1) the temperature of described roasting is 450～550 ℃.
9. described internal electrolysis of iron Preparation of catalysts method as claimed in claim 7 is characterized in that in step 2) in, the concentration of described soluble copper salt is 0.1～1.0mol/L, the concentration of described manganese salt solution is 0.1～1.0mol/L; The time of described dipping is 2～30min, and the temperature of described drying is 100～130 ℃, and the temperature of described roasting is 200～300 ℃.
10. described internal electrolysis of iron Preparation of catalysts method as claimed in claim 7 is characterized in that in step 3) described natural manganese sand particle grain size is 2～5mm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010102615233A CN101934230B (en) | 2010-08-25 | 2010-08-25 | Iron inner electrolysis catalyst and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010102615233A CN101934230B (en) | 2010-08-25 | 2010-08-25 | Iron inner electrolysis catalyst and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101934230A true CN101934230A (en) | 2011-01-05 |
| CN101934230B CN101934230B (en) | 2012-07-25 |
Family
ID=43387941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2010102615233A Expired - Fee Related CN101934230B (en) | 2010-08-25 | 2010-08-25 | Iron inner electrolysis catalyst and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101934230B (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102826646A (en) * | 2011-06-17 | 2012-12-19 | 同济大学 | Catalytic iron internal electrolysis biological fluidization filler and preparation method thereof |
| CN104150568A (en) * | 2014-09-05 | 2014-11-19 | 刘理方 | Catalytic micro-electrolysis material and preparation method thereof |
| CN107321303A (en) * | 2017-07-28 | 2017-11-07 | 滨州学院 | A kind of preparation method and applications of load Mn molecular sieves |
| CN109482864A (en) * | 2019-01-11 | 2019-03-19 | 中南大学 | A kind of iron-based implantation material of manganese dioxide catalytic degradation and preparation method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01151938A (en) * | 1987-12-08 | 1989-06-14 | Mitsubishi Heavy Ind Ltd | Deodorant |
| CN1935680A (en) * | 2005-09-19 | 2007-03-28 | 上海城市污染控制工程研究中心 | Method for treating sewage by catalytic iron internal electrogravimetry and its filler |
| CN101665311A (en) * | 2009-09-24 | 2010-03-10 | 中南大学 | Catalysis and micro-electrolysis combined technology for high-concentration refractory organic wastewater |
-
2010
- 2010-08-25 CN CN2010102615233A patent/CN101934230B/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01151938A (en) * | 1987-12-08 | 1989-06-14 | Mitsubishi Heavy Ind Ltd | Deodorant |
| CN1935680A (en) * | 2005-09-19 | 2007-03-28 | 上海城市污染控制工程研究中心 | Method for treating sewage by catalytic iron internal electrogravimetry and its filler |
| CN101665311A (en) * | 2009-09-24 | 2010-03-10 | 中南大学 | Catalysis and micro-electrolysis combined technology for high-concentration refractory organic wastewater |
Non-Patent Citations (2)
| Title |
|---|
| 《环境化学》 20020131 刘会娟等 锰砂催化电化学方法对燃料K2G脱色效果的研究 第68页第1.1部分 1-10 第21卷, 第1期 2 * |
| 《陕西科技大学学报》 20060228 Li Jian-bin Treatment of Molasses Alcohol Wastewater by Internal Electrolysis 第25页第1部分 1-10 第24卷, 第1期 2 * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102826646A (en) * | 2011-06-17 | 2012-12-19 | 同济大学 | Catalytic iron internal electrolysis biological fluidization filler and preparation method thereof |
| CN104150568A (en) * | 2014-09-05 | 2014-11-19 | 刘理方 | Catalytic micro-electrolysis material and preparation method thereof |
| CN104150568B (en) * | 2014-09-05 | 2015-12-09 | 刘理方 | A kind of catalysis and micro-electrolysis material and preparation method thereof |
| CN107321303A (en) * | 2017-07-28 | 2017-11-07 | 滨州学院 | A kind of preparation method and applications of load Mn molecular sieves |
| CN109482864A (en) * | 2019-01-11 | 2019-03-19 | 中南大学 | A kind of iron-based implantation material of manganese dioxide catalytic degradation and preparation method thereof |
| CN109482864B (en) * | 2019-01-11 | 2020-04-24 | 中南大学 | Manganese dioxide catalytic degradation iron-based implant and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101934230B (en) | 2012-07-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105457643B (en) | A kind of preparation method of activated carbon supported type catalyst for Electrocatalysis Degradation organic wastewater | |
| CN104925913B (en) | For removing catalyst particle electrode of hardly degraded organic substance and ammonia nitrogen and its preparation method and application in decontamination sewage | |
| CN109647431B (en) | Catalyst for catalytic oxidation treatment of refractory wastewater by ozone, preparation method and application thereof | |
| CN106861654B (en) | A kind of immobilization particle and its preparation and application of same for treating acidic mine wastewater | |
| CN106277278A (en) | A kind of method utilizing iron oxides multiphase Fenton system to process arsenic-containing waste water | |
| CN108993475B (en) | Ternary composite material heterogeneous light Fenton catalyst and preparation and application thereof | |
| CN102764660B (en) | Bipolar three-dimensional electrode catalyst packing and preparation method thereof | |
| CN101920188B (en) | Method for modifying manganese ore and application thereof in removal of arsenic from groundwater permeable reactive wall | |
| CN105731624A (en) | Method for treating reverse osmosis concentrated water through heterogeneous Fenton-like reaction catalytic oxidization | |
| CN102794182A (en) | Preparation method of composite ozonation solid catalyst and catalyst | |
| CN105668719A (en) | CoO loaded activated carbon catalyst particle electrode and preparation method | |
| CN101934230B (en) | Iron inner electrolysis catalyst and preparation method thereof | |
| CN108483582A (en) | A kind of nitrite efficient degradation material and its preparation method and application | |
| CN107552052B (en) | Treatment method of refractory organic wastewater | |
| CN111606519A (en) | Advanced treatment method for electroplating wastewater | |
| CN106277660A (en) | A kind of heterogeneous catalysis ozone processes the method for residual active sludge | |
| CN105540954B (en) | A kind of method that chemical denitrification removes nitrate nitrogen in water removal | |
| CN105417800B (en) | A kind of method that environmental protection removes nitrate nitrogen in waste water | |
| CN105753503A (en) | Electrocatalysis particle electrode for efficiently degrading bisphenol A in wastewater and preparation method of electrocatalysis particle electrode | |
| CN107902745B (en) | Treatment method of landfill leachate concentrated water | |
| CN102583894A (en) | Method for treating landfill leachate tail water through magnetic carbon catalyzed ozonation | |
| CN102765799B (en) | Method of chain scission for high concentration persistent organic pollutants in wastewater | |
| CN105645557A (en) | Catalytic wet air oxidation processing method of circulating water | |
| CN114230097A (en) | Treatment process of sewage containing organic phosphorus | |
| CN105712468B (en) | A method of processing waste water difficult for biological degradation |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20120725 Termination date: 20150825 |
|
| EXPY | Termination of patent right or utility model |